Colon Cancer: Gene >> LPP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000617246
Start	188872654:188872654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1601C>T
AA Mutation	p.Pro534Leu(p.P534L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000617246
Start	188609825:188609825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770028872
CDS Mutation	c.1094C>T
AA Mutation	p.Ala365Val(p.A365V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000617246
Start	188760178:188760178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1306G>T
AA Mutation	p.Val436Phe(p.V436F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000617246
Start	188866239:188866239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1450A>G
AA Mutation	p.Met484Val(p.M484V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617246
Start	188609385:188609385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754782287
CDS Mutation	c.654G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617246
Start	188524712:188524712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146490639
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617246
Start	188874356:188874356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754547383
CDS Mutation	c.1716C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000617246
Start	188609815:188609816(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1089dupC
AA Mutation	p.Cys364LeufsTer29(p.C364Lfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LPP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000617246
Start	188866258:188866258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1469C>T
AA Mutation	p.Ala490Val(p.A490V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript